An Unusual Presentation of a Chronic Lymphocytic Leukemia Patient with 17p Deletion After Reduced-Intensity Transplantation: Richter Syndrome and Concomitant Graft-Versus-Host Disease-Case Report

Salihoglu A., Ozbalak M., Keskin D., Tecimer T., Soysal T., Ferhanoglu B.

TRANSPLANTATION PROCEEDINGS, cilt.45, sa.7, ss.2845-2848, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier


Chronic lymphocytic leukemia (CLL) patients with 17p deletion comprise a challenging subgroup associated with poor overall survival. These patients should be treated with alternative strategies. Reduced-intensity conditioning (RIC) allogeneic stem cell transplantation (allo-SCT) can achieve long-term remission in this ultra-high-risk CLL group. Herein, we described a CLL patient with 17p deletion who developed Richter syndrome with extranodal involvement of the liver soon after RIC allo-SCT despite apparent acute graft-versus-host disease.